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硫酸曲古霉素对从人体分离出的支原体和脲原体的体外活性。

In-vitro activity of trospectomycin sulphate against Mycoplasma and Ureaplasma species isolated from humans.

作者信息

Yancey R J, Klein L K

机构信息

Microbiology and Nutrition Research Unit, Upjohn Company, Kalamazoo, MI 49001.

出版信息

J Antimicrob Chemother. 1988 Jun;21(6):731-6. doi: 10.1093/jac/21.6.731.

Abstract

Trospectomycin sulphate, a novel analogue of spectinomycin, was compared to spectinomycin, tetracycline, lincosamide, macrolide, quinolone and naphthalenic ansamycin-class antibiotics for in-vitro activity against Mycoplasma pneumoniae, M. hominis and Ureaplasma urealyticum. MIC determinations were conducted by the agar dilution method using either SP-4 (Mycoplasma spp.) or A8 (U. urealyticum) agars. Trospectomycin compared favorably with tetracycline for all the strains of M. pneumoniae, M. hominis or U. urealyticum tested. Ciprofloxacin was the most active of the newer quinolones tested. Trospectomycin was as active as this quinolone antibiotic, or more active, in vitro. Other antibiotics such as the macrolides and lincosamides were highly active against one or more of the three mycoplasma groups tested but none was active against all three. The results suggest that trospectomycin may be useful in the treatment of mycoplasma-induced respiratory or genital tract infections in man.

摘要

硫酸曲古霉素是壮观霉素的一种新型类似物,将其与壮观霉素、四环素、林可酰胺、大环内酯、喹诺酮和萘并安莎霉素类抗生素进行了比较,以研究它们对肺炎支原体、人型支原体和解脲脲原体的体外活性。采用琼脂稀释法,使用SP-4(支原体属)或A8(解脲脲原体)琼脂进行最低抑菌浓度(MIC)测定。对于所有测试的肺炎支原体、人型支原体或解脲脲原体菌株,硫酸曲古霉素与四环素相比表现良好。环丙沙星是所测试的新型喹诺酮类药物中活性最强的。硫酸曲古霉素在体外与这种喹诺酮类抗生素活性相当,或活性更强。其他抗生素,如大环内酯类和林可酰胺类,对所测试的三个支原体组中的一个或多个具有高活性,但没有一种对所有三个组都有活性。结果表明,硫酸曲古霉素可能对治疗人类支原体引起的呼吸道或生殖道感染有用。

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